2010
DOI: 10.1016/s1003-9953(09)60048-7
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Synthesis of ethyl acetate by esterification of acetic acid with ethanol over a heteropolyacid on montmorillonite K10

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Cited by 41 publications
(27 citation statements)
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“…49 Also, a study of this reaction with the same 2:1 molar ratio, using 30 wt.% H 3 PW/montmorillonite K10 under approximately similar experimental conditions of our report, yielded 90% ethyl acetate, but at 8 h reaction. 50 The behavior of the higher yield with excess of acetic acid was consistent to other mechanism studies in the literature. 51 It has been proposed a single-site mechanism (Eley-Riedel) in which the adsorbed carboxylic acid reacts with the alcohol (methanol or ethanol) in both gas/liquid-phase, describing the kinetics very satisfactorily.…”
Section: Resultssupporting
confidence: 78%
“…49 Also, a study of this reaction with the same 2:1 molar ratio, using 30 wt.% H 3 PW/montmorillonite K10 under approximately similar experimental conditions of our report, yielded 90% ethyl acetate, but at 8 h reaction. 50 The behavior of the higher yield with excess of acetic acid was consistent to other mechanism studies in the literature. 51 It has been proposed a single-site mechanism (Eley-Riedel) in which the adsorbed carboxylic acid reacts with the alcohol (methanol or ethanol) in both gas/liquid-phase, describing the kinetics very satisfactorily.…”
Section: Resultssupporting
confidence: 78%
“…Because of low specific area (\10 m 2 /g) and dissolution in polar solution, heteropolyacid is not easy to separate from the reaction mixture and its catalytic reaction stability is poor [11]. Through supporting heteropolyacid on SiO 2 [12,13] and other carries [14][15][16][17], or anchoring it on supports modified by organic functional groups [18][19][20], some stable heteropolyacid catalysts are obtained in many references. With the complete or partial substitution of different counter cations for protons, its leaching could also be prevented.…”
Section: Introductionmentioning
confidence: 98%
“…Different heterogeneous catalysts were tested in the esterification of acetic acid with ethanol and 2-propanol, including carbon materials [6,7], zeolites [4,5,8], aluminophosphates [9], mesoporous solids [10], heteropolyacids [11][12][13] also including group five elements [12], montmorillonite [14] or resins [15][16][17]. However, because of the nature of esterification processes the very high yield of ester is limited by reaction equilibrium.…”
Section: Introductionmentioning
confidence: 99%